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Items: 2

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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4409816copy number variation1nstd174human GRCh37 chr1: 84,388,267-84,389,032 , GRCh38.p12 chr1: 83,922,584-83,923,349 TTLL7
    esv2664430copy number variation52estd199human GRCh37 chr1: 84,388,342-84,388,953 , GRCh38.p12 chr1: 83,922,659-83,923,270 TTLL7

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